Presenter

Talia has experience in pharmaceutical clinical research, human factors usability in medical device development, risk management and US regulatory strategy that allows her to support clients to bring safe, effective, and intuitive medical devices to market. By applying the knowledge and skills obtained from years of conducting regulated clinical trials to the realm of human factors usability, she provides a unique perspective to medical device development. She understands that medical device development is an iterative process and that human factors goes hand-in-hand with risk management during product design.